EnhancerDB
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  3. rs569704934[chr16:4349941]
Enhancers that have rs569704934[chr16:4349941]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr16 4330820 4352135 enh16514
Astrocyte Colon (HCT116) Uterus Epithelial (MCF-7) Stomach Skin (Keratinocyte) Brain (SK-N-SH) Bone (Osteoblast) Thyroid Pancreas (Panc1) Neural Stem Cells (H9) Thymus Prostate (PC-3) Cervix (HeLa-S3) Large Intestine Esophagus Placenta Lung (PC-9) Muscle (Myoblast) Muscle (Myotube) Liver (HepG2) Prostate (RWPE1) Muscle (A673) Heart
Transcript factors that have rs569704934[chr16:4349941]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr16 4349798 4350262 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21686573
chr16 4349803 4350199 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21686574
chr16 4349851 4350054 ZNF274 GTRD no Liver (HepG2) 21686575
chr16 4349863 4350153 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21686576
chr16 4349900 4350100 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21686577
chr16 4349917 4350177 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21686578
chr16 4349930 4350314 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21686579
chr16 4349935 4350225 ZBTB33 ENCODE Uniform TFBS no Colon (HCT116) 21686580
Genes associated with rs569704934[chr16:4349941], comfirmed by eQTL
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Blank TSI value indicates lack of sufficient expression for calculation
Chrom. Start End Strand Gene name Ensembl ID TSS of gene Distance between TSS and SNP Tissue q Value id More